PHEX, DMP1 and FGF23 mutations in a malaysian hypophosphatemic rickets patient

Nurul Nadirah Razali; Tzer Hwu Ting; Karuppiah Thilakavathy

doi:10.7490/f1000research.1110334.1

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Razali NN, Ting TH and Thilakavathy K. PHEX, DMP1 and FGF23 mutations in a malaysian hypophosphatemic rickets patient [version 1; not peer reviewed]. F1000Research 2015, 4:587 (poster) (https://doi.org/10.7490/f1000research.1110334.1)

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PHEX, DMP1 and FGF23 mutations in a malaysian hypophosphatemic rickets patient

Nurul Nadirah Razali, Tzer Hwu Ting, Karuppiah Thilakavathy ¹

Published 20 Aug 2015 (https://doi.org/10.7490/f1000research.1110334.1)

Author Affiliations

¹ Universiti Putra Malaysia, Malaysia

Copyright © 2015 Razali NN et al. This is an open access work distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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CITE

Published 20 Aug 2015

PHEX, DMP1 and FGF23 mutations in a malaysian hypophosphatemic rickets patient
[version 1; not peer reviewed]

Nurul Nadirah Razali, Tzer Hwu Ting, Karuppiah Thilakavathy ¹

Author Affiliations

¹ Universiti Putra Malaysia, Malaysia

Presented at

7th International Conference on Children's Bone Health 2015

Abstract

Competing Interests

No competing interests were disclosed

Keywords

Hypophosphatemic rickets, PHEX, DMP1, FGF23

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PHEX, DMP1 and FGF23 mutations in a malaysian hypophosphatemic rickets patient

PHEX, DMP1 and FGF23 mutations in a malaysian hypophosphatemic rickets patient [version 1; not peer reviewed]

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PHEX, DMP1 and FGF23 mutations in a malaysian hypophosphatemic rickets patient
[version 1; not peer reviewed]